Famotidine

Product NDC

0378-3020

11-digit product format

003783020

Labeler code

0378

Product ID

0378-3020_3d598544-4d57-4875-b685-99a108270be4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

famotidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA075704

Marketing category

ANDA

Marketing start

2001-04-16

Marketing end

2020-02-29

Substance

FAMOTIDINE

Active strength

20 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record